AU3419399A - Novel process for the fermentative production of cephalosporin - Google Patents

Novel process for the fermentative production of cephalosporin

Info

Publication number
AU3419399A
AU3419399A AU34193/99A AU3419399A AU3419399A AU 3419399 A AU3419399 A AU 3419399A AU 34193/99 A AU34193/99 A AU 34193/99A AU 3419399 A AU3419399 A AU 3419399A AU 3419399 A AU3419399 A AU 3419399A
Authority
AU
Australia
Prior art keywords
mixture
complex mixture
adipyl
cephalosporin
general formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
AU34193/99A
Inventor
Ilco Adrianus Lambertus Antonius Boogers
Dick Schipper
Emilius Johannes Albertus Xaveriu Van De Sandt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Koninklijke DSM NV
Original Assignee
DSM NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by DSM NV filed Critical DSM NV
Publication of AU3419399A publication Critical patent/AU3419399A/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P35/00—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin
    • C12P35/08—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin disubstituted in the 7 position
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/02—Preparation
    • C07D501/12—Separation; Purification
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/182—Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system
    • C12P17/183—Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system containing an indolo[4,3-F,G]quinoleine nucleus, e.g. compound containing the lysergic acid nucleus as well as the dimeric ergot nucleus
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/185—Heterocyclic compounds containing sulfur atoms as ring hetero atoms in the condensed system
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/188—Heterocyclic compound containing in the condensed system at least one hetero ring having nitrogen atoms and oxygen atoms as the only ring heteroatoms
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P35/00—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Cephalosporin Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)

Abstract

A method for the recovery of an N-substituted cephalosporanic acid compound of general formula (I), wherein R2 is selected from the group consisting of adipyl (1,4-dicarboxybutane), succinyl, glutaryl, adipyl, pimelyl, suberyl, 2-carboxyethyithio)acetyl, 3-carboxyethylthio)propionyl, higher alkyl saturated and higher alkyl unsaturated dicarboxylic acids, from a complex mixture comprising in addition to the compound of general formula (I) 6-aminopenicillanic acid (6-APA) and optionally one or more N-substituted penicillanic acid compounds, comprising the steps of: (a) acidifying the complex mixture to a pH below 6.5 and maintaining the mixture below said pH at a temperature of between 10° C. and 150° C.; and/or (b) contacting the complex mixture with a carbon dioxide source; and (c) recovering the cephalosporanic acid compound of formula (I) from the mixture obtained after steps (a) and/or (b).
AU34193/99A 1998-03-27 1999-03-26 Novel process for the fermentative production of cephalosporin Abandoned AU3419399A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP98201011 1998-03-27
EP98201011 1998-03-27
PCT/EP1999/002247 WO1999050271A1 (en) 1998-03-27 1999-03-26 Novel process for the fermentative production of cephalosporin

Publications (1)

Publication Number Publication Date
AU3419399A true AU3419399A (en) 1999-10-18

Family

ID=8233541

Family Applications (1)

Application Number Title Priority Date Filing Date
AU34193/99A Abandoned AU3419399A (en) 1998-03-27 1999-03-26 Novel process for the fermentative production of cephalosporin

Country Status (17)

Country Link
US (2) US6552185B1 (en)
EP (1) EP1066294B1 (en)
JP (1) JP2002509933A (en)
KR (1) KR100594774B1 (en)
CN (1) CN1138781C (en)
AT (1) ATE226954T1 (en)
AU (1) AU3419399A (en)
BR (1) BR9909108A (en)
DE (1) DE69903719T2 (en)
ES (1) ES2186347T3 (en)
ID (1) ID26888A (en)
PL (1) PL343099A1 (en)
PT (1) PT1066294E (en)
RU (1) RU2219182C2 (en)
SI (1) SI1066294T1 (en)
WO (1) WO1999050271A1 (en)
ZA (1) ZA200004801B (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2186347T3 (en) * 1998-03-27 2003-05-01 Dsm Nv NEW PRODUCTION PROCEDURE FOR FERMENTATION OF CEPHALOSPORINE.
ATE267831T1 (en) * 1999-09-30 2004-06-15 Otsuka Kagaku Kk CRYSTALS OF CEPHEM DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF
JP2002316991A (en) * 2001-04-18 2002-10-31 Otsuka Chem Co Ltd Penicillin and cephalosporin compound
CN1912130B (en) * 2005-08-08 2011-06-15 百瑞全球有限公司 Two-step enzyme method for preparing 7-aminocephalosporanic acid
CN103108879B (en) * 2010-09-07 2016-08-17 中化帝斯曼制药有限公司荷兰公司 For the method producing cephalosporins
EP3666074A1 (en) * 2018-12-16 2020-06-17 Sandoz GmbH Adjuvant composition, method of producing the adjuvant composi-tion and uses thereof
CN112625053B (en) * 2020-12-30 2022-08-09 伊犁川宁生物技术股份有限公司 7-ACA with low content of maximum unknown simple impurity and preparation method thereof

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE465649A (en) * 1944-06-19
GB810196A (en) * 1955-02-02 1959-03-11 Nat Res Dev Cephalosporin c
GB1272769A (en) * 1968-08-02 1972-05-03 Glaxo Lab Ltd Improvements in or relating to cephalosporin derivatives
FR2404642A1 (en) * 1977-09-29 1979-04-27 Roussel Uclaf NEW DERIVATIVE OF CEPHALOSPORIN C, PROCESS FOR PREPARATION AND APPLICATION OF THE NEW PRODUCT TO THE PREPARATION OF 7-AMINO CEPHALOSPORANIC ACID
US5318896A (en) * 1991-09-11 1994-06-07 Merck & Co., Inc. Recombinant expandase bioprocess for preparing 7-aminodesacetoxy cephalosporanic acid (7-ADCA)
KR100227711B1 (en) 1991-10-15 1999-12-01 한스 발터 라벤 Novel bioprocesses for preparing 7-aca and 7-adac
DE69434023D1 (en) 1993-07-30 2004-10-28 Dsm Ip Assets Bv Process for the efficient production of 7-ADCA via 2- (carboxyethylthio) acetyl-7-ADCA and 3- (carboxymethylthio) propionyl-7-ADCA
BE1009070A3 (en) * 1995-02-02 1996-11-05 Dsm Nv PROCESS FOR THE EXTRACTION OF A beta-lactam drug.
AU3661597A (en) * 1996-07-29 1998-02-20 Bristol-Myers Squibb Company Solvent extraction of 3-hydroxymethylcephalosporins
BE1010651A3 (en) * 1996-09-27 1998-11-03 Dsm Nv Process for the purification of cefalexin.
BR9804855A (en) 1997-04-22 1999-08-24 Gist Brocades Bv Perfect process for fermentative cephalosporin production
ES2186347T3 (en) * 1998-03-27 2003-05-01 Dsm Nv NEW PRODUCTION PROCEDURE FOR FERMENTATION OF CEPHALOSPORINE.

Also Published As

Publication number Publication date
RU2219182C2 (en) 2003-12-20
PT1066294E (en) 2003-03-31
ES2186347T3 (en) 2003-05-01
ZA200004801B (en) 2001-07-25
DE69903719D1 (en) 2002-12-05
ID26888A (en) 2001-02-15
JP2002509933A (en) 2002-04-02
EP1066294A1 (en) 2001-01-10
WO1999050271A1 (en) 1999-10-07
US6803460B2 (en) 2004-10-12
PL343099A1 (en) 2001-07-30
CN1138781C (en) 2004-02-18
CN1295575A (en) 2001-05-16
ATE226954T1 (en) 2002-11-15
US20030139595A1 (en) 2003-07-24
KR100594774B1 (en) 2006-07-03
SI1066294T1 (en) 2003-04-30
US6552185B1 (en) 2003-04-22
DE69903719T2 (en) 2003-09-18
EP1066294B1 (en) 2002-10-30
KR20010034700A (en) 2001-04-25
BR9909108A (en) 2000-12-12

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Legal Events

Date Code Title Description
MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase